General Electric Co.

GE LOGIQ I COMAPACT ULTRASOUND, GE LOGIQ E COMPACT ULTRASOUND, GE VIVID E COMPACT ULTRASOUND

All identifiers (2)

Aletia (canonical)ALT-002003

FDA 510(k) · US (primary)K072797

Regulatory Registrations

🌐

FDA

ID: K072797

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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